Canonical Allele Identifier: PA915981324
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164693
ClinVar Variation Id: 2995600
ClinVar RCV Id: RCV003853687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly1298Arg
CA278722
NM_001127180.2:c.3892G>A
CA381947894
NM_001127180.2:c.3892G>C